209 results on '"Felicetti L"'
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2. Calibration and testing strategies to correct atmospheric effects on star tracking algorithms
3. Dust impact and attitude analysis for JAXA’s probe on the Comet Interceptor mission
4. Modeling Approaches for Simulating Molecular Communications
5. Modified dynamic programming for asteroids belt exploration
6. Modeling Approaches for Simulating Molecular Communications
7. A reaction-null/Jacobian transpose control strategy with gravity gradient compensation for on-orbit space manipulators
8. Nanosatellite swarm missions in low Earth orbit using laser propulsion
9. A Hybrid Formulation for Modelling Multibody Spacecraft
10. The Mechanism of Protein Synthesis Activation after Fertilization of Sea Urchin Eggs
11. Sequence homology between 4qter and 10qter loci facilitates the instability of subtelomeric Kpn (ital) I repeat units implicated in facioscapulohumeral muscular dystrophy
12. Chromosome 4q35 haplotypes and DNA rearrangements segregating in affected subjects of 19 Italian families with facioscapulohumeral musculatur dystrophy (FSHD)
13. Fast collision detection for nanosimulators
14. Directional Receivers for Diffusion-Based Molecular Communications
15. Direct detection of 4q35 rearrangements implicated in facioscapulohumeral muscular dystrophy (FSHD)
16. Molecular characterization of β-thalassemia mutations in Egypt
17. PFGE analysis of 4qter-10qter interchromosomal exchanges in Italian families with Facioscapulohumeral muscular dystrophy (FSHD)
18. High frequency of 4qter-10qter subtelomeric exchanges in Italian families with Facioscapulohumeral muscular dystrophy (FSHD)
19. le emergenze mediche nello studio odontoiatrico- Dossier
20. Design guidelines for a space manipulator for debris removal
21. Applications of molecular communications to medicine: A survey
22. Italian experience regarding the prevention of Duchenne and Becker muscular dystrophies
23. A simulation tool for nanoscale biological communication systems
24. A case of hereditary persistence of fetal hemoglobin caused by a gene not linked to the β-globin cluster
25. A report on 528 intragenic deletions detected in DMD and BMD patients by an Italian collaborative study
26. Screening molecolare di mutazioni puntiformi nel gene alfa-globinico mediante DHPLC
27. Identificazione della curva tensione-deformazionedi acciai sulla base di prove di durezza strumentate
28. A simulation tool for nanoscale biological networks
29. Modeling the formationkeeping control with multibody codes
30. Isotopic and gross fecal analysis of American black bear scats
31. Glycogenic acanthosis presenting as leukoplakia on the tongue
32. P22 Incidence of oral squamous sarcinoma in an Italian population of patients with oral lichen planus
33. P148 Static cytometry and classic G-banding cytogenetic procedures are both effective In detecting genetic alterations in oral pre-neoplastic lesions
34. P151 Cell-turnover is not related to the presence/absence of tissue inflammation in oral lesions at different risk of developing squamous carcinoma
35. P152 Predictive role of p53 protein as a single marker or associated to Ki67 antigen in oral carcinogenesis
36. P150 Evaluation of the cell turn-over in the clinically and histologically normal tumor-distant mucosa and in the corresponding primary oral carcinoma
37. Predictive Role of p53 Protein as a Single Marker or Associated to Ki67 Antigen in Oral Carcinogenesis
38. Changes in motor cortex excitability in facioscapulohumeral muscular dystrophy
39. Molecular characterization of HbH disease in the Cuban population
40. Progress in the molecular diagnosis of facioscapulohumeral muscular dystrophy and correlation between the number ofKpnI repeats at the 4q35 locus and clinical phenotype
41. Molecular analysis of 4q35 rearrangements in facioscapulohumeral muscular dystrophy (FSHD): application to family studies for a correct genetic advice and a reliable prenatal diagnosis of the disease
42. Sequence Homology between 4qter and 10qter Loci Facilitates the Instability of Subtelomeric KpnI Repeat Units Implicated in Facioscapulohumeral Muscular Dystrophy
43. Asymptomatic dystrophinopathies: analysis of DNA, mRNA and protein
44. Molecular mechanism of DNA rearrangements implicated in FSH dystrophy and applications to the diagnosis of the disease
45. Sickle cell anemia and β‐gene cluster haplotypes in Cuba
46. Analysis of β-thalassemia mutations in the United Arab Emirates provides evidence for recurrent origin of the IVSINT 5 (G-C) mutation
47. 4q35 molecular probes for the diagnosis and genetic counseling of facioscapulohumeral muscular dystrophy
48. A new β‐thalassaemia frameshift mutation detected by PCR after selective hybridization to immobilized oligonucleotides
49. 242 Breakpoints in the 200-kb deletion-prone P20 region of the DMD gene are widely spread
50. Variable hypomethylation of D4Z4 in facioscapulohumeral muscular dystrophy.
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